Canonical Allele Identifier: CA1590915558
Gene: TCOF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.150371826_150371827delinsCT , CM000667.2:g.150371826_150371827delinsCT GRCh38
NC_000005.9:g.149751389_149751390delinsCT , CM000667.1:g.149751389_149751390delinsCT GRCh37
NC_000005.8:g.149731582_149731583delinsCT NCBI36
NG_011341.1:g.19188_19189delinsCT

Transcript Alleles

HGVS Amino-acid change
ENST00000427724.7:c.640-180_640-179delinsCT ENSP00000390717.3:n.640-180_640-179delinsCT
ENST00000513538.2:c.640-180_640-179delinsCT ENSP00000422567.2:n.640-180_640-179delinsCT
ENST00000643257.2:c.640-180_640-179delinsCT MANE Select ENSP00000493815.1:n.640-180_640-179delinsCT
ENST00000643812.1:c.779-180_779-179delinsCT ENSP00000493833.1:n.779-180_779-179delinsCT
ENST00000646961.1:c.639+2224_639+2225delinsCT ENSP00000496754.1:n.639+2224_639+2225delinsCT
ENST00000650162.1:c.639+2224_639+2225delinsCT ENSP00000497075.1:n.639+2224_639+2225delinsCT
ENST00000323668.11:c.639+2224_639+2225delinsCT ENSP00000325223.6:n.639+2224_639+2225delinsCT
ENST00000377797.7:c.640-180_640-179delinsCT ENSP00000367028.4:n.640-180_640-179delinsCT
ENST00000394269.7:c.640-180_640-179delinsCT ENSP00000377811.3:n.640-180_640-179delinsCT
ENST00000427724.6:c.640-180_640-179delinsCT ENSP00000390717.2:n.640-180_640-179delinsCT
ENST00000439160.6:c.640-180_640-179delinsCT ENSP00000406888.2:n.640-180_640-179delinsCT
ENST00000445265.6:c.639+2224_639+2225delinsCT ENSP00000409944.2:n.639+2224_639+2225delinsCT
ENST00000504761.6:c.640-180_640-179delinsCT ENSP00000421655.2:n.640-180_640-179delinsCT
ENST00000513346.5:c.640-180_640-179delinsCT ENSP00000427484.1:n.640-180_640-179delinsCT
ENST00000515035.5:n.1405-180_1405-179delinsCT
ENST00000515516.1:c.342+3909_342+3910delinsCT ENSP00000426471.1:n.342+3909_342+3910delinsCT
NM_000356.3:c.639+2224_639+2225delinsCT NP_000347.2:n.639+2224_639+2225delinsCT
NM_001008657.2:c.640-180_640-179delinsCT NP_001008657.1:n.640-180_640-179delinsCT
NM_001135243.1:c.640-180_640-179delinsCT NP_001128715.1:n.640-180_640-179delinsCT
NM_001135244.1:c.640-180_640-179delinsCT NP_001128716.1:n.640-180_640-179delinsCT
NM_001135245.1:c.639+2224_639+2225delinsCT NP_001128717.1:n.639+2224_639+2225delinsCT
NM_001195141.1:c.640-180_640-179delinsCT NP_001182070.1:n.640-180_640-179delinsCT
XM_005268502.2:c.640-180_640-179delinsCT XP_005268559.1:n.640-180_640-179delinsCT
XM_005268503.2:c.640-180_640-179delinsCT XP_005268560.1:n.640-180_640-179delinsCT
XM_005268504.2:c.640-180_640-179delinsCT XP_005268561.1:n.640-180_640-179delinsCT
XM_005268505.2:c.640-180_640-179delinsCT XP_005268562.1:n.640-180_640-179delinsCT
XM_005268506.2:c.640-180_640-179delinsCT XP_005268563.1:n.640-180_640-179delinsCT
XM_005268507.2:c.639+2224_639+2225delinsCT XP_005268564.1:n.639+2224_639+2225delinsCT
XM_005268508.2:c.640-180_640-179delinsCT XP_005268565.1:n.640-180_640-179delinsCT
XM_005268509.2:c.640-180_640-179delinsCT XP_005268566.1:n.640-180_640-179delinsCT
XM_011537678.1:c.640-180_640-179delinsCT XP_011535980.1:n.640-180_640-179delinsCT
XR_427778.1:n.685-180_685-179delinsCT
XR_427779.1:n.685-180_685-179delinsCT
XR_427780.1:n.685-180_685-179delinsCT
XM_005268502.4:c.640-180_640-179delinsCT XP_005268559.1:n.640-180_640-179delinsCT
XM_005268503.4:c.640-180_640-179delinsCT XP_005268560.1:n.640-180_640-179delinsCT
XM_005268504.4:c.640-180_640-179delinsCT XP_005268561.1:n.640-180_640-179delinsCT
XM_005268505.4:c.640-180_640-179delinsCT XP_005268562.1:n.640-180_640-179delinsCT
XM_005268506.4:c.640-180_640-179delinsCT XP_005268563.1:n.640-180_640-179delinsCT
XM_005268507.4:c.639+2224_639+2225delinsCT XP_005268564.1:n.639+2224_639+2225delinsCT
XM_005268508.4:c.640-180_640-179delinsCT XP_005268565.1:n.640-180_640-179delinsCT
XM_005268509.4:c.640-180_640-179delinsCT XP_005268566.1:n.640-180_640-179delinsCT
XM_011537678.3:c.640-180_640-179delinsCT XP_011535980.1:n.640-180_640-179delinsCT
XM_017009792.2:c.640-180_640-179delinsCT XP_016865281.1:n.640-180_640-179delinsCT
XM_017009793.2:c.640-180_640-179delinsCT XP_016865282.1:n.640-180_640-179delinsCT
XM_017009794.2:c.640-180_640-179delinsCT XP_016865283.1:n.640-180_640-179delinsCT
XM_017009795.2:c.639+2224_639+2225delinsCT XP_016865284.1:n.639+2224_639+2225delinsCT
XR_427778.3:n.687-180_687-179delinsCT
XR_427779.2:n.687-180_687-179delinsCT
XR_427780.3:n.687-180_687-179delinsCT
NM_000356.4:c.639+2224_639+2225delinsCT NP_000347.2:n.639+2224_639+2225delinsCT
NM_001008657.3:c.640-180_640-179delinsCT NP_001008657.1:n.640-180_640-179delinsCT
NM_001135244.2:c.640-180_640-179delinsCT NP_001128716.1:n.640-180_640-179delinsCT
NM_001135245.2:c.639+2224_639+2225delinsCT NP_001128717.1:n.639+2224_639+2225delinsCT
NM_001195141.2:c.640-180_640-179delinsCT NP_001182070.1:n.640-180_640-179delinsCT
NM_001371623.1:c.640-180_640-179delinsCT MANE Select NP_001358552.1:n.640-180_640-179delinsCT
NM_001135243.2:c.640-180_640-179delinsCT NP_001128715.1:n.640-180_640-179delinsCT